Package 16571-774-50

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 16571-774-50
Digits Only 1657177450
Product NDC 16571-774
Product ID 16571-774_f06a97e3-4349-4df3-87de-4479c1ed69bc
Description

500 TABLET in 1 BOTTLE (16571-774-50)

Marketing

Marketing Status
Marketed Since 2012-06-29
Brand glimepiride
Generic glimepiride
Sample Package No

Linked Drug Pages (1)

Glimepiride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f06a97e3-4349-4df3-87de-4479c1ed69bc", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0316571774012", "0316571773015", "0316571775019"], "unii": ["6KY687524K"], "rxcui": ["199245", "199246", "199247"], "spl_set_id": ["48ada723-8144-497d-afd6-a8c52a1dd3ff"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-774-01)", "package_ndc": "16571-774-01", "marketing_start_date": "20120629"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16571-774-50)", "package_ndc": "16571-774-50", "marketing_start_date": "20120629"}], "brand_name": "Glimepiride", "product_id": "16571-774_f06a97e3-4349-4df3-87de-4479c1ed69bc", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "16571-774", "generic_name": "Glimepiride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "2 mg/1"}], "application_number": "ANDA202759", "marketing_category": "ANDA", "marketing_start_date": "20120629", "listing_expiration_date": "20271231"}